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Sinus Histiocytosis With Massive Lymphadenopathy Involving the Orbit
, 1998 Sharon Goldberg +3 more
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Sinus Histiocytosis with Massive Lymphadenopathy
Annals of Otology, Rhinology & Laryngology, 1989Sinus histiocytosis with massive lymphadenopathy is a lymphoreticular disorder of obscure pathogenesis with extranodal lesions and a variable clinical course. Clinical manifestations are most often in the head and neck, with 97% of patients showing cervical lymphadenopathy and a significant but lesser number having lesional infiltrates in the upper ...
Nour Sneige, John G. Batsakis
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Sinus Histiocytosis with Massive Lymphadenopathy
Clinical Nuclear Medicine, 1987Gallium uptake corresponding to the extent of the disease in a patient with histologically proven sinus histiocytosis with massive lymphadenopathy (SHML) is reported. Computerized tomography confirmed the presence of bilateral retrobulbar masses, involvement of both lateral recti, erosion of the bony orbital floor with encroachment of tumor into the ...
Stanley H. Weiss, Behram Pastakia
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SINUS HISTIOCYTOSIS WITH MASSIVE LYMPHADENOPATHY
Acta Paediatrica, 1977Abstract Brostrøm, K. and Baandrup, U. (University Department of Paediatrics and University Institute of Pathology, Kommunehospitalet, Aarhus, Denmark). Sinus histiocytosis with massive lymphadenopathy. Acta Paediatr Scand, 66:257, 1977.—The present case report brings to attention an unusual form of massive benign lymphadenopathy which can simulate ...
U. Baandrup, K. Brostrøm
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Brucellosis and sinus histiocytosis with massive lymphadenopathy
The American Journal of Medicine, 1989S inus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a benign pseudolymphomatous entity with distinct clinical and pathologic features [l-3]. This disorder, usually occurring during the first two decades of life, is manifested by massive, painless cervical lymphadenopathy in association with fever, leukocytosis ...
Peter M. Banks +3 more
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Sinus histiocytosis with massive lymphadenopathy: A “massive” misnomer
Diagnostic Cytopathology, 2014Sinus histiocytosis with massive lymphadenopathy also known as Rosai–Dorfman disease is a rare, benign, histiocytic disorder of unknown origin characterized by lymphadenopathy. Since its original description by Rosai and Dorfman in 1969, small number of cases has been reported; hence no specific diagnostic criteria and treatment guidelines have been ...
Divesh Sardana +2 more
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Sinus histiocytosis with massive lymphadenopathy
Archives of Orthopaedic and Trauma Surgery, 1993A 64-year-old female patient has been suffering from sinus histiocytosis with massive lymphadenopathy (SHML) for 2 years. After 12 months of illness, the patient developed swelling and pain in various skeletal regions. Scintigraphic, radiological and CT imaging revealed multiple osseous lesions.
Andreas Eisenschenk +3 more
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The neurologic manifestations of sinus histiocytosis with massive lymphadenopathy
Neurology, 1982Sinus histiocytosis with massive lymphadenopathy is a benign pseudolymphomatous disease with distinctive microscopic features. Painless cervical adenopathy is the most characteristic clinical finding, although other node groups and extranodal sites may be involved. Of 200 patients in a case registry, 8 had neurologic symptoms.
Russell K. Brynes +3 more
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SINUS HISTIOCYTOSIS WITH MASSIVE LYMPHADENOPATHY PRESENTING AS A MENINGIOMA
Neuropathology and Applied Neurobiology, 1987Sinus histiocytosis with massive lymphadenopathy presenting as a meningiomaThis report documents a case of sinus histiocytosis with massive lymphadenopathy (SHML) which was unusual in that it produced a localized mass on the intracranial dura, simulating a meningioma. The clinical, histological and ultrastructural features of this case are presented.
C P Case, M P Carey
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The Osseous Manifestations of Sinus Histiocytosis with Massive Lymphadenopathy
American Journal of Clinical Pathology, 1981The cases of five patients who had sinus histiocytosis with massive lymphadenopathy accompanied by osseous involvement by the disease are presented. Four of the five patients were children. The bone lesions were multiple in four cases and solitary in one.
Patrick D. Walker +2 more
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